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IOSR Journal of Dental and Medical Sciences (IOSR-JDMS)

e-ISSN: 2279-0853, p-ISSN: 2279-0861.Volume 13, Issue 12 Ver. IV (Dec. 2014), PP 72-73
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A Rare Dual Ovarian Tumor Mucinous Cystadenoma with Adult


Granulosa Cell Tumor
Dr.Rooplata1, Dr.Yerramsetti Ananthalakshmi2
1. 3rd year PG. Department of OBG, Raja rajeshwari Medical College and Hospital .
2. Assistant Professor, Department of Surgery, Konaseema Institute of Medical Sciences
and Research Foundation.

Abstract: Dual tumor in an ovary is a rare entity and combination of mucinous cystadenoma with adult
granulosa cell tumor (GCT) is very rare. Dual tumor represents a coexistence of two adjacent tumors but
histologically distinct tumors without admixture in the same tissue or organ. Mucinous neoplasms occur rarely
in association with granulosa cell tumor. GCT is low-grade malignancy and need a close follow up for
recurrences which may be late. Here we present a case in 39 year old female who presented outpatient
department with complaints of lower abdomen pain and dysfunctional uterine bleeding. Patient underwent
hysterectomy with salphingo oophorectomy and specimen sent for histopathological examination, where it was
diagnosed as mucinous cystadenoma in association with Adult granulosa cell tumor.
Key Words: Dual tumor, ovary, Mucinous Cystadenoma, Granulosa cell tumor.

I.

Introduction

Adult granulosa cell tumor (GCT) accounts for 1-2% of all ovarian neoplasm and they are known for
late recurrences, even after 10-20 years in some cases.[1] Mucinous neoplasms occur rarely in association with
granulosa cell tumor, cystic teratoma, Sertolileydig cell tumor and carcinoid tumor. [2] Dual tumors represent a
coexistence of two adjacent but histologically distinct tumors without admixture in the same tissue or organ.
Here we report a rare case of dual tumor comprising of mucinous cystadenoma in association with granulosa
cell tumor in a 39 year old woman.

II.

Case Report

Here we present a case of 39 year old female who presented outpatient department with complaints of
lower abdomen pain and with irregular bleeding per vagina since six months. Ultra sonography findings showed
a mass in the right ovary measuring 18x12 cms predominantly solid mass. Patient underwent hysterectomy with
salphingo oophorectomy and specimen sent for histopathological examination, where it was diagnosed as
mucinous cystadenoma in association with Adult granulosa cell tumor.
Gross Findings
The specimen showed enlarged right ovary measuring 18 x 12 cms. The cut section of the ovary
showed both solid and cystic areas.
Microscopic Findings
microscopically the sections studied showed features of both solid and cystic component. The solid
component was highly cellular with closely packed sheets of cells, cells are round to oval cells lobulated by
fibrous Septa. Cells showed eosinophilic cytoplasm and relatively uniform pale nuclei with prominent grooves.
Call-Exner bodies were present at places as Adult granulosa cell tumor [figure 1] and cystic component showed
that it was lined by a single layer of uniform mucin- filled tall columnar cells with basal nuclei, resembling
endocervical epithelium, the features which were consistent with mucinous cystadenoma.[figure2].

III.

Discussion

Dual tumors in an ovary represent a coexistence of two adjacent tumors but histologically distinct
tumors without admixture in the same tissue or organ. Dual tumors in ovary are a rare entity and combination of
mucinous cystadenoma and adult granulosa cell tumor is very rare. Though dual tumors in ovary have been
reported earlier, like serous cystadenoma and mature cystic teratoma, [3] but combined mucinous cystadenoma
and GCT was rarely reported. GCT and mucinous cystadenoma are independent tumor arising from sex cord
stromal cells and surface epithelium of ovary, respectively.
Adult granulosa cell tumor (GCT) accounts for 1-2% of all ovarian neoplasm and they are known for
late recurrences, even after 10-20 years in some cases.[1] In the present case grossly it was cystic and there was
small solid foci, which microscopically showed features of GCT and cystic component showed features of
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A Rare Dual Ovarian Tumor: Mucinous Cystadenoma With Adult Granulosa Cell Tumor
mucinous cystadenoma. Occasionally GCT presents as a small lesion in cystic teratoma which could easily be
missed through inadequate sections, so ovaries with mature cystic teratoma should be examined thoroughly for
small foci of GCT. [4]
Dual tumors have been described in various organs including oesophagus, stomach, liver, bone, kidney,
brain and lung, such tumors involving the ovary are rare. At a molecular level, various cytogenetic abnormalities
have been discovered in adult GCT. Trisomy 12 and 14, monosomy 22 are among the more prevalent ones.
Aneuploidy has been correlated with a poorer survival. In addition, germ line P53 mutations have also been
reported in these tumors. The prognostic significance of this mutation is, however, not known. Further research
is needed before a definite conclusion is drawn regarding the clinical significance of these cytogenetic markers.
[5,6]
To conclude, we would like to emphasize upon the fact that multiloculated cysts have to be extensively
examined grossly, so as not to miss any solid component which might have a bearing on prognosis of the
patient. However; in the present case the small solid foci showed the
features of GCT. GCT tumors are characterized by a very indolent course, and late recurrences.
This association of GCT and mucinous cystadenoma warrants close follow up of patient
as recurrences can occur many years after removal of primary tumor.

References
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Russell P. surface epithelial stromal tumors of ovary. In: Kurman RJ, ed. Blausteins pathology of the female genital tract. 4 th ed.
New York: Springer-Verlag, 1994;724.
Ozgur B, Ahmet D, Meral KC, Mustafa S, Cagnur U et al. Collision tumor: serous cystadenoma and dermoid cyst in the same
ovary. Archives of gynaecology and obstetrics 2009;279:767-70.
Dgani R, Rozenman D, Lifschitz-Mercer B. Granulosa cell tumorarising in an ovary with mature cystic teratoma. Int J Gynaecol
Obstet1993;3:287-9.
Mayr D, Kaltz WC, Arbogast S et al. characteristic pattern of genetic aberrations in ovarian granulosa cell tumors. Mod Pathol
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unusual germline p53 mutation. Mod Pathol 2004;17:868-73.

Figure 1: round to oval cells with eosinophilic cytoplasm and prominent nuclear grooves. (H&E X400)

Figure 2: cystic component lined by a single row of uniform mucin-filled tall columnarcells with basal nuclei
(H&E X 100)

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